Canonical Allele Identifier: PA205016
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 210003
ClinVar RCV Id: RCV000191944 RCV001514042 RCV002287389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.Lys4732Thr
CA205015
NM_001256071.3:c.14195A>C